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Journal of Virology, July 2008, p. 7135-7143, Vol. 82, No. 14
0022-538X/08/$08.00+0     doi:10.1128/JVI.00448-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Intersubunit Disulfide Isomerization Controls Membrane Fusion of Human T-Cell Leukemia Virus Env{triangledown}

Kejun Li,1 Shujing Zhang,1 Malin Kronqvist,1 Michael Wallin,1 Maria Ekström,1 David Derse,2 and Henrik Garoff1*

Department of Biosciences and Nutrition, Karolinska Institute, S-141 57 Huddinge, Sweden,1 HIV Drug Resistance Program, National Cancer Institute, Frederick, Maryland2

Received 29 February 2008/ Accepted 3 May 2008

Human T-cell leukemia virus (HTLV-1) Env carries a typical disulfide isomerization motif, C225XXC, in the C-terminal domain SU. Here we have tested whether this motif is used for isomerization of the intersubunit disulfide of Env and whether this rearrangement is required for membrane fusion. We introduced the C225A and C228A mutations into Env and found that the former but not the latter mutant matured into covalently linked SU-TM complexes in transfected cells. Next, we constructed a secreted Env ectodomain and showed that it underwent incubation-dependent intersubunit disulfide isomerization on target cells. However, the rearrangement was blocked by the C225A mutation, suggesting that C225 carried the isomerization-active thiol. Still, it was possible to reduce the intersubunit disulfide of the native C225A ectodomain mutant with dithiothreitol (DTT). The importance of the CXXC-mediated disulfide isomerization for infection was studied using murine leukemia virus vectors pseudotyped with wild-type or C225A HTLV-1 Env. We found that the mutant Env blocked infection, but this could be rescued with DTT. The fusion activity was tested in a fusion-from-within assay using a coculture of rat XC target and transfected BHK-21 effector cells. We found that the mutation blocked polykaryon formation, but this could be reversed with DTT. Similar DTT-reversible inhibition of infection and fusion was observed when a membrane-impermeable alkylator was present during the infection/fusion incubation. We conclude that the fusion activity of HTLV-1 Env is controlled by an SU CXXC-mediated isomerization of the intersubunit disulfide. Thus, this extends the applicability of the isomerization model from gammaretroviruses to deltaretroviruses.

* Corresponding author. Mailing address: Department of Biosciences and Nutrition, Karolinska Institute, S-141 57 Huddinge, Sweden. Phone: 46-8-6089125. Fax: 46-8-7745538. E-mail: henrik.garoff{at}cbt.ki.se

{triangledown} Published ahead of print on 14 May 2008.

Journal of Virology, July 2008, p. 7135-7143, Vol. 82, No. 14
0022-538X/08/$08.00+0     doi:10.1128/JVI.00448-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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